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Hans R Waterham

Showing results (21-30 of 223) with videos related to

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Biochimica Et Biophysica Acta|January 18, 2011
Inhibition of the isoprenoid biosynthesis pathway; detection of intermediates by UPLC-MS/MSLinda Henneman, Arno G van Cruchten, Willem Kulik, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderJeannette Gootjes, Frank Schmohl, Hans R Waterham, et al.
Histochemistry and Cell Biology|December 26, 2016
Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell lineFemke C C Klouwer, Janet Koster, Sacha Ferdinandusse, et al.
Arthritis and Rheumatism|November 1, 2006
A role for geranylgeranylation in interleukin-1beta secretionSaskia H L Mandey, Loes M Kuijk, Joost Frenkel, et al.
Clinical Dysmorphology|January 7, 2003
Midface hypoplasia, obesity, developmental delay and neonatal hypotonia in two brothersLieke Rozendaal, Harry Del Canho, Hans R Waterham, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 18, 2024
Molecular and cellular consequences of mevalonate kinase deficiencyFrouwkje A Politiek, Marjolein Turkenburg, Linda Henneman, et al.
Human Mutation|October 31, 2009
Spectrum of PEX6 mutations in Zellweger syndrome spectrum patientsMerel S Ebberink, Janet Kofster, Ronald J A Wanders, et al.
Human Mutation|July 13, 2006
Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiencySaskia H L Mandey, Marit S Schneiders, Janet Koster, et al.
Clinical Rheumatology|December 16, 2006
A patient with hyper-IgD syndrome responding to anti-TNF treatmentErkan Demirkaya, M Kazim Caglar, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|December 22, 2023
Identification of FDA-approved drugs that increase mevalonate kinase in hyper IgD syndromeFrouwkje A Politiek, Marjolein Turkenburg, Janet Koster, et al.
Pageof 23

Showing results (21-30 of 223) with videos related to

Sort By:
Pageof 23
Biochimica Et Biophysica Acta|January 18, 2011
Inhibition of the isoprenoid biosynthesis pathway; detection of intermediates by UPLC-MS/MSLinda Henneman, Arno G van Cruchten, Willem Kulik, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderJeannette Gootjes, Frank Schmohl, Hans R Waterham, et al.
Histochemistry and Cell Biology|December 26, 2016
Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell lineFemke C C Klouwer, Janet Koster, Sacha Ferdinandusse, et al.
Arthritis and Rheumatism|November 1, 2006
A role for geranylgeranylation in interleukin-1beta secretionSaskia H L Mandey, Loes M Kuijk, Joost Frenkel, et al.
Clinical Dysmorphology|January 7, 2003
Midface hypoplasia, obesity, developmental delay and neonatal hypotonia in two brothersLieke Rozendaal, Harry Del Canho, Hans R Waterham, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 18, 2024
Molecular and cellular consequences of mevalonate kinase deficiencyFrouwkje A Politiek, Marjolein Turkenburg, Linda Henneman, et al.
Human Mutation|October 31, 2009
Spectrum of PEX6 mutations in Zellweger syndrome spectrum patientsMerel S Ebberink, Janet Kofster, Ronald J A Wanders, et al.
Human Mutation|July 13, 2006
Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiencySaskia H L Mandey, Marit S Schneiders, Janet Koster, et al.
Clinical Rheumatology|December 16, 2006
A patient with hyper-IgD syndrome responding to anti-TNF treatmentErkan Demirkaya, M Kazim Caglar, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|December 22, 2023
Identification of FDA-approved drugs that increase mevalonate kinase in hyper IgD syndromeFrouwkje A Politiek, Marjolein Turkenburg, Janet Koster, et al.
Pageof 23